Mixture of esters of para amino benzoic acid and ascorbic acid

ABSTRACT

A solution of L-ascorbic acid and a solution of para amino benzoic acid are mixed and the mixture evaporated to permit recovery of a solid compound. The compound is administered to a host to reduce thrombotic tendencies.

OTHER APPLICATIONS

This application is a continuation of Ser. No. 317,763, filed Nov. 3, 1981, abandoned, which is a division of Ser. No. 117,066, Jan. 31, 1980, now U.S. Pat. No. 4,329,290, which in turn, is a continuation-in-part of Ser. No. 35,637, filed May 3, 1979, abandoned, which, in turn, is a continuation of Ser. No. 701,874, July 1, 1976, now U.S. Pat. No. 4,164,585.

FIELD OF INVENTION

This invention relates to compounds of organic acids and to methods of making and using the same particularly for pharmaceutical purposes.

BACKGROUND OF THE INVENTION

U.S. Pat. No. 3,722,504 describes a screen for testing pharmaceutical compounds based at least partly on their ability to increase the negative surface charge of the vascular system. U.S. Pat. No. 3,722,504, by way of example, discloses a pharmaceutical compound which prevents thrombosis by modifying the intimal surface charge of the vascular system.

Para amino benzoic acid increases the net negative surface charge of blood vessels and blood cells. It produces marked increases in the current induced occlusion time in rat mesentary vessels (see U.S. Pat. No. 3,956,504). It produces no measurable effect on blood coagulation studies. It has a limited effect on blood vessel wall pores as shown by electro-osmotic studies.

Para amino benzoic acid, further, has good antithrombotic characteristics but tends to have relative little anti-coagulant activity as shown by its lack of effect on the coagulation studies including partial thromboplastin time, thrombin time and recalcification time. It is therefore a very useful antithrombotic drug.

Para amino benzoic acid has various very significant properties as a drug:

1. It is inexpensive;

2. It is known to be non-toxic in humans;

3. It can be used for long periods of time without significant incidence of pathological manifestations.

4. The material can be taken orally in large dosages without significant toxicity.

In man, dosages have been administered, for example, as high as 12 to 24 grams a day without significant side effects. It has furthermore been used for a large number of diseases in man including the therapy of Ricketsial diseases before the development of anti-biotics, for tuberculosis in very large dosage and in the treatment of certain protozoan diseases and other infestation. It has long been thought to be a mild anti-inflammatory agent.

In humans with arteriosclerotic peripheral vascular disease, para amino benzoic acid has been shown to increase blood flow in ischemic limbs as measured by Barcroft plethysmographic studies and Doppler blood flow measurements. Studies which were carried out in approximately fifty patients resulted in an approximate doubling of blood flows in patients in which para amino benzoic acid salt was effective. U.S. Pat. No. 3,956,504 has been issued on the effect of para amino benzoic acid on blood flow in man.

The long term effects of vitamin C on scurvy in man is a primary event of historical interest in medicine. The effects of vitamin C to prevent scurvy are extraordinarily well documented throughout the world. Man, deprived of vitamin C for periods longer than approximately sixty days, starts to display evidence of capillary fragility and bleeding into all tissues and organs. Vitamic C has the following characteristics:

1. It is a co-enzyme in the Kreb's cycle.

2. It is a reducing agent and electron donor in 11 known biological systems.

L-ascorbic acid or vitamin C has a variety of biological functions some of which are not completely understood (Zitent et al 1964). Large doses of L-ascorbic acid appear to have value in prevention and symptom reduction in the common cold and other viral diseases (Linus Pauling 1974). Recent experimental evidence indicates that L-ascorbic acid is effective in reducing serum cholesterol levels. C. Spittle (The Lancet, July 28, 1973; pp. 199-201 and Dec. 11, 1971; pp. 1280-1281) suggested that dosages of 1 to 2 grams of vitamin C per day can be beneficial in the prevention of deep vein thrombosis as well as in reducing the incidence of atherosclerotic complications in man. Recent research indicates that ascorbic acid may reduce the incidence of myocardial infarction (Knox, E. G., The Lancet, pp. 1465, June 30, 1973). L-ascorbic acid, further, appears to offset the thrombogenic effects of oral contraceptives as demonstrated by prolongation of occlusion times in the mesenteric vessels.

Good results were obtained in a pilot study using seven volunteer subjects to determine the effects of ascorbic acid on (1) plasma coagulation characteristics (2) serum cholesterol levels (3) platelet aggregability and (4) surface charge characteristics of red cells and platelets. Vitamin C in these subjects was shown to decrease platelet aggregability and increase the electro-phoretic mobility of all the tested cells.

There has been little evidence to indicate that vitamin C effects measured blood coagulability as demonstrated by partial thromboplastin time, thrombin times and thrombin recalcification times.

Spittle et al have tested vitamin C in a randomized group of patients with thrombophlebitis. The protective effect of vitamin C against thrombosis has been shown by a randomized double-blind trial using patients who were shown to be prone to deep-venous thrombosis. In a total of fifty-three patients, it was observed that the incidence of deep venous thrombosis was 33% in patients dosed with L-ascorbic acid compared to 60% in the placebo group (Spittle, C. R., The Lancet, pp. 199, July 28, 1973). The dose given was 1 gram per day. This correlation between the intake of vitamin C and reduction in the number of thrombotic episodes has been confirmed by other sources. In burn patients, where it is customary to use large doses of vitamin C to speed healing, there has been an apparent demand for treatment of deep-vein thrombosis. This information is based on the experience of one hospital over a five and one-half year period during which time 159 patients over forty years of age were treated with large doses of vitamin C (Spittle, C. R., "The Action of Vitamin C on Blood Vessels," Amer. Heart J. 88: 387, 1974).

A combination of para amino benzoic acid and vitamin C has been shown, for example, in Runti, I1 Farmaco, Ed. Sci., Vol. X, 1955, pp. 424-431.

SUMMARY OF THE INVENTION

It is an object of the invention to provide an improved combination of para amino benzoic acid and L-ascorbic acid.

It is another object of the invention to provide an improved pharmaceutical compound having improved utility for extended periods following administration.

Yet another object of the invention is to provide improved methods for the treatment of hosts and the prevention of vascular conditions.

Still another object is to promote the development of useful compounds based on organic acids and the like.

A further object of the invention is to provide new methods for the development of pharmaceutical compounds.

To achieve the above and other objects of the invention, there is provided a method comprising reducing thrombotic tendencies in a host by administering to the host a compound derived from two organic acids.

According to one embodiment of the invention, one of the acids is L-ascorbic acid and the other is para amino benzoic acid.

The compound which is derived may be a salt or ester and this compound may be administered in a dosage of 1-100 mg./kg. of body weight. The dosage is preferably administered orally, although it can be administered interperitoneally.

The compound may be formed by mixing solutions of L-ascorbic acid and various forms of para amino benzoic acid and recovering the thusly resulting solid.

The invention includes, as one aspect thereof, compounds prepared according to the above method or specifically salts and esters of L-ascorbic acid and para amino benzoic acid to obtain: ##STR1##

BRIEF DESCRIPTION OF DRAWING

The sole FIGURE of the drawing is a chart demonstrating the prolonged activity of dosages of the compound of the invention.

DETAILED DESCRIPTION

Hereinabove, reference had been made to para amino benzoic acid. The formula for this organic acid is as follows: ##STR2##

Reference has also been made to L-ascorbic acid or vitamin C, the formula for which is: ##STR3##

The present invention relates to compounds derived from these organic acids, namely, salts, esters and amides thereof, the synthesization of the same and the applicability thereof to the treatment of the vascular system, notably in rats, dogs and human hosts requiring such treatment.

The formula for the salt of our earlier U.S. Pat. No. 4,164,585 is as follows: ##STR4##

The original approach was to prepare a salt of ascorbic acid with para amino benzoic acid. Such a salt can be shown in two forms--one using the open form of ascorbic acid, the other using the enol form.

Two manufacturing procedures used are described below. Because of the ease of oxidation of ascorbic acid, it is essential to perform all operations under nitrogen and free of water and air. In one case, substantial darkening of the product resulted. It was believed this was due to the presence of moisture.

EXAMPLE I

1. A solution of para mino benzoic acid in a mixture of 50% acetone and 50% methanol was prepared with gentle heating. The concentration was approximately 100 grams per liter.

2. A similar solution was prepared with L-ascorbic acid.

3. The two solutions were mixed. Water was excluded to the extent possible.

4. The mixture was evaporated under vacuum, with nitrogen being utilized to flush the system. As the material concentrated, crystals began to appear.

5. When the solution was evaporated, until it was a thick slurry, the material was filtered through a coarse filter paper and allowed to drain as dry as possible. The surface was blanketed with nitrogen, with great care to exclude all filtered water.

6. The resultant solid was dried under high vacuum at room temperature. The ratio of L-ascorbic acid to para amino benzoic acid used was one to one on a molar basis.

EXAMPLE II

1. An alternative method of preparation used was to evaporate the solvent with careful exclusion of water and air to the point where a solid semi-dry cake was obtained in the container in which the evaporation was conducted.

2. This moist cake was then transferred to an appropriate container and dried under high vacuum. All operations are protected against exposure to air and moisture.

Other solvent systems will undoubtedly work. The above were used largely as a matter of convenience. An odor develops in the process which is removed with high vacuum drying, but must represent a by-product which is formed during the process. It must also be volatile, since it can be removed.

The first salt shown above, theoretically, only requires the removal of a molecule of water to form the amide. In general, this does not happen too readily. The distillation of the solvents may help pull off water.

Initial studies were directed toward determining the toxicity of the above-indicated compound in mammalia.

A very high dosage per kilogram of body weight in rats and dogs has been shown essentially non-toxic.

The new compound was next tested to determine its effect on rat-mesentery occlusion studies. Half lives of para amino benzoic acid have been shown to approximate one day. Half lives of vitamin C approximate 12 hours to a maximum of 1 day. The half lives of the new compound have been shown to approximate 4 to 5 days with a tail. A single dose lasts approximately 14 days. Mechanical mixing of para amino benzoic acid and L-ascorbic acid have been shown to have a maximal tail of approximately 5 to 6 days indicating by direct logic that the new compound is biologically different from the two components mixing together mechanically. Specifically, the compound derived appears to be more potent than the starting materials mixed together in a 50/50 ratio. If the agents are mixed together in the same ratio as used when making the new compound, the mechanical mixture is still not as potent as the compound derived.

The new compound has been evaluated in rat-mesentery studies. In the rat-mesentery, the new compound has been shown to prolong coagulation 3 to 4 times the normal rat-mesentery thrombosis time. The result is dramatic and prolonged since the effect of a single dose appears to extend out to 14 days before rat-mesentery occlusion times return to a normal level. This result is based on 26 rats.

Blood cells of male dogs fed with the new compound display an increase in negative surface charge which increases sequentially from the third day to approximately the 14th day, so that at 14 days there is a doubling of electrophoretic mobility over the effects seen on the fifth, sixth and seventh day.

The available evidence suggests that, as with most normal pharmacologic agents, the new compound will not produce super normality. It will, however, return toward normal any grossly abnormal measurements concerning the electrokinetic characteristics of blood cells and blood vessels in dogs.

The available evidence indicates that the new compound derived from L-ascorbic acid and para amino benzoic acid is a rather potent anti-thrombotic agent. Its effect is cumulatively greater than the effect of either of its components even when they are mechanically mixed together and given orally to rats and/or dogs. The compound is an elegant example of an electron donor compound which is useful in treating the vascular system.

The following are some results of tests comparing the new compound with a mixture of the starting materials and with the starting materials individually:

                                      TABLE I                                      __________________________________________________________________________     Dosages - Oral Route                                                                  RANGE MGS/KG/DAY                                                                            DURATION                                                   MATERIAL                                                                              Minimum                                                                              Maximum                                                                               ADMINISTRATION                                                                            TOXICITY EFFECT                                 __________________________________________________________________________     PABA (X)                                                                              1     10     Indefinite Low cutaneous                                                                           Relatively                                                            manifestation.                                                                          limited                                L-Ascorbic                                                                            0.25  10     Indefinite Low cutaneous                                                                           Critical in                            Acid (Y)                                                                              mgs.                    manifestation.                                                                          maintenance                                                           Gastritis. Some                                                                         of tissue                                                             evidence dis-                                                                           integrity                                                             turbence gene                                                                           particularly                                                          pool in massive                                                                         vascular tree                                                         dosage. Catalytic                                                              oxidizer Krebs                                                                 cycle essential                                                                vitamins.                                       X + Y  1     100 mg/kg                                                                             Unknown    Very low gas-                                                                           Prolonged rat                          (mixture)    rats   long term  tritis in one                                                                           mesentery                                                             rat, in high                                                                            occlusion                                                             dosage 1 mg/gm                                                                          time. Single                                                          body weight                                                                             dose run                                                              dosage.  (day 1):                                                                       170 ± 20 min.                                                               Tail - 7 days.                         X - Y  2     100 mg/kg                                                                             May be     Very low Prolonged.                             (compound)          given long gastritis.                                                                              Longer tail                                                term                than X + Y                                                                     Tail - 14 days                                                                 Occlusion                                                                      time:                                                                          206 = 24 min.                          __________________________________________________________________________      X - Y tail  minimum 14 days in experimental animals                            X + Y tail  minimum 7 days in experimental animals                       

The following additional data was obtained relative to the utility of the new compound:

    ______________________________________                                         EFFECT OF NEW COMPOUND ON ELECTRICALLY IN-                                     DUCED THROMBOSIS IN RAT MESENTERIC VESSELS                                     ______________________________________                                         SINGLE LOADING DOSE                                                            20 mg/100 g B.W.    MALE                                                       MELTING POINT - 147° C.                                                 1 DAY AFTER SINGLE LOADING DOSE                                                1 Rat    The occlusion time was 240 minutes                                    3 DAYS AFTER SINGLE LOADING DOSE                                               1 Rat    The occlusion time was 150 minutes                                    2 Rat    The occlusion time was 195 minutes                                    ______________________________________                                    

The following data relates to rat-mensentery occlusion time:

    ______________________________________                                         RAT-MESENTERY OCCLUSION TIME                                                                 OCCLUSION                                                                      TIME      CONTROL                                                ______________________________________                                         PABA                                                                           35 mg p.o./d × 3 d (F)                                                                   95 min (1F) 45 + 5 min (3F)                                    35 mg p.o./d × 3 d (M)                                                                   53 ± 13 min                                                                 (7M)                                                           L-ASCORBIC ACID                                                                10 mg/100 g body weight/                                                                       112 ± 18 min                                                                            45 ± 5 min (2F)                                 per day × 3 days (F)                                                                     (5F)                                                           10 mg/100 g body weight/                                                                       135 ± 14 min                                                                            38 ± 10 min (3M)                                per day × 3 days (M)                                                                     (2M)                                                           PABA +                                                                         L-ASCORBIC ACID                                                                35 mg + 10 mg/100 g body                                                                       108 ± 23.0 min                                                                          45 ± 5 min (2F)                                 weight          (6F)                                                                           128 ± 18.0 min                                                                          38 ± 10 min (3M)                                                (2M)                                                           10 mg + 10 mg   160 min (2F)                                                                               50 minutes (1F)                                    (3M + 3F)       175 min (3M)                                                                               55 minutes (1M)                                                    AF + 3M                                                        PABA -          1 day                                                          L-ASCORBIC ACID after Single                                                   SALT            Loading Dose                                                   (NEW COMPOUND)  240 min (1F)                                                   20 mgs/100 grams                                                                               3 days                                                                         after Single                                                                   Loading Dose                                                                   150 min (1M)                                                                   195 min (2F)                                                   ______________________________________                                    

The following data relates to the occlusion time tail in female rats:

    ______________________________________                                         (X - Y) - NEW COMPOUND - SINGLE DOSE/P.O.                                      100 mg/100 g body weight                                                                         Average Occluding Time                                       ______________________________________                                         1 day             206 ± 24.0 min (5F)                                       5 days            143 ± 9.5 min (5F)                                        9 days            137 ± 12.0 min (5F)                                       11 days           127 ± 34.0 min (4F)                                       14 days            67 ± 4.5 min (4F)                                                          Control - 48 ± 1.1 min (5F)                               ______________________________________                                    

Below are tabulated some physical characteristics of batches of the compound which were made:

    ______________________________________                                                 MELTING POINT                                                                              SOLUBILITY                                                 ______________________________________                                         Batch 1   157° C.                                                                               Sparingly Soluble;                                                             1 gm/100 cc. H.sub.2 O                                 Batch 2   157° C.                                                                               Same                                                   Batch 3   147° C.                                                                               Same                                                   ______________________________________                                    

Referring next to the sole FIGURE of the drawing, it is seen that there are illustrated the effects of a single loading dose on a number of rats. A control is provided in the form of five animals and it is noted from the chart in the drawing that the control provides a rat-mesentery occlusion time relative to electrically-induced thrombosis which is, at the outset, less than a single loading dose of the new compound after 14 days.

More particularly, it will be noted that five animals were sacrificed after one day following administration of the new compound, five animals were sacrificed after five days, five more animals were sacrificed after nine days, four additional animals were sacrificed after 11 days and finally, four animals were sacrificed after 14 days. The occlusion time (in minutes) after the first day is markedly greater than that of the controls. After five days, the occlusion time is reduced but is still more than double that of the controls. Similarly, after nine days, the occlusion time is substantially greater than the controls and has reduced only very slightly from the fifth day measurements. Similarly, after 11 days, there is very little reduction in occlusion time which is still at least twice as great as that of the controls. After 14 days, measurement of four sacrificed animals still reveals an occlusion time which is greater than that of the controls. reveals an occlusion time which is greater than that of the controls.

The measurements in the drawing are based upon an administration of the compound in a dosage of 100 mg/100 g of body weight and single loading doses are employed for both the controls and the animals to which the new compound has been administered. This shows a substantial tail inures to the benefit of administration of the new compound and this is important with respect to the treatment of humans wherein oral administration of the new compound is expected to lead to a scheduled administration which provides for spaced-oral dosages over a period of days, such as, for example, one oral administration per week.

The following additional compounds have been made for the above utility:

EXAMPLE III

An antithrombotic compound is prepared in the form of the salt of glyceryl p-aminobenzoate and ascorbic acid. The structure is: ##STR5##

Method of Preparation

This salt was prepared by dispersing equal molar portions of the two substances in a mixture of methanol and acetone. The mixture is heated until everything is in true solution. The solvent is then evaporated until precipitation begins. At that point the mixture is chilled. The salt which crystalizes out is then collected and dried in vacuum. The characteristics of the molecule are as follows:

Melting point--117°-152° C. (brioad range probably reflects salt tendency to decompose rather than give a clean melting point).

The NMR and IR curves of the salt appear to be different from the NMR and IR curves of the individual components, indicating a new molecule is present.

EXAMPLE IV

An antithrombotic compound is prepared in the form of the salt of ethyl p-aminobenzoate and ascorbic acid. The structure is: ##STR6##

Method of Preparation

The method is identical to that for the ethyl p-aminobenzoate salt.

Melting point--88°-168° C. (brioad range reflects salt decomposition).

The IR and NMR analyses show unique spectral differences from the component compounds.

EXAMPLE V

An antithrombotic compound is prepared in the form of esters of p-aminobenzoic acid with ascorbic acid. A mixture of esters consisting of more than one of the following structures has been prepared. IR and NMR data have been obtained to show the presence of ester bonding. Thin layer chromatography shows the presence of more than one component. The structures for esters are: ##STR7##

Method of Preparation

The esters were prepared by reacting p-nitrobenzoyl chloride with ascorbic acid in a solvent with a basic component chloride acceptor present, such as pyridine or triethanolamine. By reacting these materials under reflux conditions, esterfication occurs with the release of hydrochloric acid, as shown in the following schema.

p-nitrobenzoyl chloride+ascorbic acid

mono-ester(s)+HCl

di-ester(s)+HCl

tri-ester+3HCl

After the isolation by evaporation of the solvents, the nitroesters are reacted with suitable reducing agents, which will only reduce the nitro group. These include zinc and hydrochloric acid and lithium aluminum borohydride. Other reducing agents could be used.

The new compounds were isolated by evaporation of the solvent. Removal of all color was accomplished by treatment of the solvent solution with activated carbon. The product is a mixture of some or all of the esters of p-aminobenzoic acid with ascorbic acid.

There will now be obvious to those skilled in the art, many modifications and variations of the above methods and compounds. These modifications and variations will not depart from the scope of the invention if defined by the following claims or if generally equivalent thereto. 

What is claimed is:
 1. A mixture of esters of para amino benzoic acid and ascorbic acid.
 2. The mixture of claim 1 wherein the esters are two or more esters of para amino benzoic acid selected from the group consisting of and ascorbic acid: ##STR8##
 3. The mixture of claim 1 wherein the esters are two or more esters of para amino benzoic acid and ascorbic acid selected from the group consisting of: ##STR9##
 4. The mixture of claim 1 wherein the esters are produced by reacting para nitrobenzoyl chloride with ascorbic acid in a suitable solvent to obtain nitro esters; isolating the nitro esters; and reducing the nitro groups to obtain the mixture of esters.
 5. The mixture of claim 4 wherein the nitro groups are reduced by a reducing agent of zinc, hydrochloric acid, or lithium aluminum borohydride.
 6. The mixture of claim 4 wherein the solvent is pyridine or triethanolamine.
 7. The mixture of claim 2 wherein the esters are produced by reacting para nitrobenzoyl chloride with ascorbic acid in a solvent of pyridine or triethanolamine to obtain nitro esters and subsequently reducing the nitro groups with a reducing agent.
 8. The mixture of claim 7 wherein the nitro groups are reduced by a reducing agent of zinc, hydrochloric acid, or lithium aluminum bromide.
 9. The mixture of claim 3 wherein the esters are produced by reacting para nitro benzoyl chloride with ascorbic acid in a solvent of pyridine or triethanol amine to obtain nitro esters and reducing the nitro groups with a reducing agent.
 10. The mixture of claim 9 wherein the nitro groups are reduced by a reducing agent of zinc, hydrochloric acid, or lithium aluminum bromide.
 11. A mixture of esters of para amino benzoic acid and ascorbic acid produced by reacting para nitrobenzoyl chloride with ascorbic acid in a solvent of pyridine or triethanolamine to obtain nitro esters, isolating the nitro esters, and reducing the nitro groups with zinc, hydrochloric acid, or lithium aluminum borohydride to obtain the mixture of esters. 